Non-invasive imaging holds significant potential for implementation in tissue engineering. It can e.g. be used to monitor the localization and function of tissue-engineered implants, as well as their resorption and remodelling. Thus far, however, the vast majority of efforts in this area of research have focused on the use of ultrasmall super-paramagnetic iron oxide (USPIO) nanoparticle-labeled cells, colonizing the scaffolds, to indirectly image the implant material. Reasoning that directly labeling scaffold materials might be more beneficial (enabling imaging also in case of non-cellularized implants), more informative (enabling the non-invasive visualization and quantification of scaffold degradation) and more easy to translate into the clinic (since cell-free materials are less complex from a regulatory point-of-view), we here prepared three different types of USPIO nanoparticles, and incorporated them both passively and actively (via chemical conjugation; during collagen crosslinking) into collagen-based scaffold materials. We furthermore optimized the amount of USPIO incorporated into the scaffolds, correlated the amount of entrapped USPIO with MR signal intensity, showed that the labeled scaffolds are highly biocompatible, demonstrated that scaffold degradation can be visualized using MRI and provided initial proof-of-principle for the in vivo visualization of the scaffolds. Consequently, USPIO-labeled scaffold materials seem to be highly suitable for image-guided tissue engineering applications.

Photoacoustics is a powerful biomedical imaging and detection technique, because it is a noninvasive, nonionizing, and low‐cost method facilitating deep tissue penetration. However, suitable contrast agents need to be developed to increase the contrast for in vivo imaging. Gold nanoparticles are often discussed as potential sonophores due to their large absorption cross‐section and their tunable plasmon resonance. However, disadvantages such as toxicity and low photoacoustic efficiency in the tissue transparency window prevail, preventing their clinical application. As a result, there remains a strong need to develop colloidal photoacoustic contrast agents which absorb in the tissue transparency window, exhibit high photoacoustic signal, and are biocompatible. Here, a facile synthetic approach is presented to produce melanin shells around various gold nanoparticle geometries, from spheres to stars and rods. These hybrid particles show excellent dispersability, better biocompatibility, and augmented photoacoustic responses over the pure melanin or pristine gold particles, with a rod‐shape geometry leading to the highest performance. These experimental results are corroborated using numerical calculations and explain the improved photoacoustic performance with a thermal confinement effect. The applicability of melanin coated gold nanorods as gastrointestinal imaging probes in mouse intestine is showcased.

The physical or chemical integration of ultrasmall superparamagnetic iron oxide nanoparticles into the 3D collagen‐based scaffold matrix of tissue‐engineered implants by T. Lammers and co‐workers on page 754 allows highly sensitive visualization and monitoring using MRI, and enables the longitudinal assessment of implant localization, function, remodeling, and resorption. Labeled scaffolds are shown to be highly biocompatible and suitable for tissue engineering applications.